KZA — Device, Vein Location, Liquid Crystal Class I
FDA product code KZA covers "Device, Vein Location, Liquid Crystal", a Class I medical device regulated under 21 CFR 880.6970. Submissions are reviewed by the General Hospital panel. At least 6 recent 510(k) clearances have been granted under this product code.
Classification Details
- Product Code
- KZA
- Device Class
- Class I
- Regulation Number
- 880.6970
- Submission Type
- Review Panel
- HO
- Medical Specialty
- General Hospital
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K152088 | novarix limited | IV-eye | February 24, 2016 |
| K101838 | vuetek scientific | VTS1000 | February 18, 2011 |
| K042679 | infrared imaging systems | IR VIEWER | December 10, 2004 |
| K982612 | ironmaster | ESP7 VENOUS IMAGE | December 14, 1998 |
| K780883 | harco products | E-Z-JECTOR | August 10, 1978 |
| K780884 | harco products | HYPO-GRIP | August 10, 1978 |